Polymerase chain reaction in high surface-to-volume ratio SiO2 microstructures

被引:42
作者
Krishnan, M
Burke, DT
Burns, MA [1 ]
机构
[1] Univ Michigan, Dept Chem Engn, Dept Human Genet, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
关键词
D O I
10.1021/ac0488356
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have performed the Taqman beta-actin PCR system in high-surface-to-volume ratio (0.02-0.13 mum(-1)) SiO2 microchannels and observed the reaction yield and uniformity. The concentrations of the enzyme, magnesium chloride, and reaction template were varied in the reaction mix, and PCR amplification was performed in devices of various surface-to-volume ratios. We found that microchannels with higher surface-to-volume ratios required higher enzyme concentrations to achieve the same amplification efficiency. We investigated the possibility that the observed reaction nonuniformity was related to the specific adsorption of magnesium ions to the negatively charged SiO2 surface. The effect of several modifications to the reaction chemistry, the addition of the caged-magnesium dye DM-Nitrophen, the replacement of human DNA template with PCR product, and the coating of the microchannel surface with Teflon were all studied. These modifications resulted in improved reaction uniformity in the microchannels and present opportunities for further studies on enhancing the efficiency and uniformity of PCR in high surface-to-volume ratio SiO2 microchannels.
引用
收藏
页码:6588 / 6593
页数:6
相关论文
共 18 条
[1]   Infectious disease - PCR detection of bacteria in seven minutes [J].
Belgrader, P ;
Benett, W ;
Hadley, D ;
Richards, J ;
Stratton, P ;
Mariella, R ;
Milanovich, F .
SCIENCE, 1999, 284 (5413) :449-450
[2]   An integrated nanoliter DNA analysis device [J].
Burns, MA ;
Johnson, BN ;
Brahmasandra, SN ;
Handique, K ;
Webster, JR ;
Krishnan, M ;
Sammarco, TS ;
Man, PM ;
Jones, D ;
Heldsinger, D ;
Mastrangelo, CH ;
Burke, DT .
SCIENCE, 1998, 282 (5388) :484-487
[3]   Formation of gradients of proteins on surfaces with microfluidic networks [J].
Caelen, I ;
Bernard, A ;
Juncker, D ;
Michel, B ;
Heinzelmann, H ;
Delamarche, E .
LANGMUIR, 2000, 16 (24) :9125-9130
[4]   Chip PCR .2. Investigation of different PCR amplification systems in microfabricated silicon-glass chips [J].
Cheng, J ;
Shoffner, MA ;
Hvichia, GE ;
Kricka, LJ ;
Wilding, P .
NUCLEIC ACIDS RESEARCH, 1996, 24 (02) :380-385
[5]   Microchannel wall coatings for protein separations by capillary and chip electrophoresis [J].
Doherty, EAS ;
Meagher, RJ ;
Albarghouthi, MN ;
Barron, AE .
ELECTROPHORESIS, 2003, 24 (1-2) :34-54
[6]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030
[7]   DETECTION OF SPECIFIC POLYMERASE CHAIN-REACTION PRODUCT BY UTILIZING THE 5'-]3' EXONUCLEASE ACTIVITY OF THERMUS-AQUATICUS DNA-POLYMERASE [J].
HOLLAND, PM ;
ABRAMSON, RD ;
WATSON, R ;
GELFAND, DH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7276-7280
[8]   Nanoliter scale PCR with TaqMan detection [J].
Kalinina, O ;
Lebedeva, I ;
Brown, J ;
Silver, J .
NUCLEIC ACIDS RESEARCH, 1997, 25 (10) :1999-2004
[9]   Chemical amplification: Continuous-flow PCR on a chip [J].
Kopp, MU ;
de Mello, AJ ;
Manz, A .
SCIENCE, 1998, 280 (5366) :1046-1048
[10]   Single-molecule DNA amplification and analysis in an integrated microfluidic device [J].
Lagally, ET ;
Medintz, I ;
Mathies, RA .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :565-570